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The Study Coordinator has overall responsibility for oversight of day to day activities during the course of the study through active coordination of all involved functions. These positions will focus primarily on Toxicology studies.
Study Coordinator
Coordinate client study activities based on study protocols and according to regulatory guidelines
Assists Study Directors in designing, conducting and reporting preclinical studies
Assists Study Director with QA audit responses
Ability to conduct a broad range of study procedures without supervision and the ability to troubleshoot experimental problems when necessary
Continually work to adapt and improve systems (e.g. experimental data collection, study conduct etc.) to make them more efficient and effective
Draft deviation and protocol amendments
QC study protocols and/or reports
Prepare raw data notebooks and pertinent records, and ensure these records are in compliance with applicable federal guidelines
Requirements:
Prefer at least 2 years’ experience as a lab tech in a CRO environment (in vivo)
Minimum of a BA or equivalent years of experience
High degree of technical proficiency
High level of attention to detail and familiarity with variety of study types
Working knowledge of Provantis
Ability to work efficiently under tight time constraints and as a member of a team
